Canonical Allele Identifier: CA371456733
Gene: CNGB3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.87751930G>C (hg19) chr8:g.86739702G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86739702G>C , CM000670.2:g.86739702G>C GRCh38
NC_000008.10:g.87751930G>C , CM000670.1:g.87751930G>C GRCh37
NC_000008.9:g.87821046G>C NCBI36
NG_016980.1:g.8974C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000320005.6:c.164C>G MANE Select ENSP00000316605.5:p.Thr55Ser
ENST00000681746.1:c.164C>G ENSP00000505959.1:p.Thr55Ser
ENST00000320005.5:c.164C>G ENSP00000316605.5:p.Thr55Ser
ENST00000519777.1:n.146C>G
NM_019098.4:c.164C>G NP_061971.3:p.Thr55Ser
NM_019098.5:c.164C>G MANE Select NP_061971.3:p.Thr55Ser
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Search 100 bp 3'